Coupling hydrogen evolution reaction (HER) with biomass valorization using a photoelectrochemical (PEC) system presents a promising approach for effectively converting solar energy to chemical energy. A crucial biomass valorization reaction is the production of value-added 2,5-furandicarboxylic acid (FDCA) via 5-Hydroxymethylfurfural (HMF) oxidation reaction (HMFOR). To achieve efficient FDCA production, we demonstrate an effective photoanode strategy that combines metal silicidation, dopant segregation, and surface reconstruction to create a bimetallic silicide NiPtSi/n-Si photoanode. The oxide-free NiPtSi/n-Si interface prepared by the metal-silicidation process ensures efficient interfacial charge transport, while dopant segregation enhances the Schottky barrier height and photovoltage, and surface reconstruction dramatically improves the catalytic activity of the photoanode surface. The as-prepared NiPtSi/n-Si photoanode exhibited excellent PEC performance for HMFOR with high conversion of HMF (97.2 %) and yield of FDCA (80.3 %) under illumination. Furthermore, by integrating a surface reconstructed NiPtSi/n-Si photoanode with a NiPtSi/p-Si photocathode, a dual-photoelectrode system was constructed capable of simultaneous production of FDCA and H, which achieves high photocurrent density of 5 mA cm at zero bias under illumination. This study offers an auspicious prospect for high cost-effectiveness conversion from solar energy to industrial monomers.
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http://dx.doi.org/10.1002/asia.202401284 | DOI Listing |
RSC Adv
December 2024
School of Materials Science and Engineering, Gwangju Institute of Science and Technology 123 Cheomdangwagi-ro, Buk-gu Gwangju 61005 Republic of Korea
Photoelectrochemical water splitting is a promising technology for converting solar energy into chemical energy. For this system to be practically viable, the materials and processes employed for photoelectrode fabrication should be cost-effective and scalable. Herein, we report the large-scale fabrication of nickel oxide-coated n-type silicon (n-Si) photoanodes chemical bath deposition for efficient photoelectrochemical water oxidation.
View Article and Find Full Text PDFChem Asian J
November 2024
Key Laboratory of Photochemical Conversion and Optoelectronic Materials, Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing 100190, China.
Coupling hydrogen evolution reaction (HER) with biomass valorization using a photoelectrochemical (PEC) system presents a promising approach for effectively converting solar energy to chemical energy. A crucial biomass valorization reaction is the production of value-added 2,5-furandicarboxylic acid (FDCA) via 5-Hydroxymethylfurfural (HMF) oxidation reaction (HMFOR). To achieve efficient FDCA production, we demonstrate an effective photoanode strategy that combines metal silicidation, dopant segregation, and surface reconstruction to create a bimetallic silicide NiPtSi/n-Si photoanode.
View Article and Find Full Text PDFNat Commun
July 2024
Institute of Fundamental and Frontier Sciences, University of Electronic Science and Technology of China, Chengdu, China.
The buried interface tens of nanometers beneath the solid-liquid junction is crucial for photocarrier extraction, influencing the overall efficiency of photoelectrochemical devices. Precise characterization of the interfacial properties is essential for device optimization but remains challenging. Here, we directly probe the in situ transformation of a CuO interlayer at the NiO/n-Si interface by hard X-ray photoelectron spectroscopy.
View Article and Find Full Text PDFACS Appl Mater Interfaces
July 2024
Department of Chemical and Biomolecular Engineering, University of California Berkeley, Berkeley, California 94720, United States.
A metal-insulator-semiconductor (MIS) structure holds great potential to promote photoelectrochemical (PEC) reactions, such as water splitting and CO reduction, for the storage of solar energy in chemical bonds. The semiconductor absorbs photons, creating electron-hole pairs; the insulator facilitates charge separation; and the metal collects the desired charge and facilitates its use in the electrochemical reaction. Despite these attractive features, MIS photoelectrodes are significantly limited by their photovoltage, a combination of the voltage generated from photon absorption minus the potential drop across the insulator.
View Article and Find Full Text PDFNatl Sci Rev
April 2024
Key Laboratory of Photochemistry, CAS Research/Education Center for Excellence in Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.
The water oxidation half-reaction at anodes is always considered the rate-limiting step of overall water splitting (OWS), but the actual bias distribution between photoanodes and cathodes of photoelectrochemical (PEC) OWS cells has not been investigated systematically. In this work, we find that, for PEC cells consisting of photoanodes (nickel-modified -Si [Ni/-Si] and α-FeO) with low photovoltage ( < 1 V), a large portion of applied bias is exerted on the Pt cathode for satisfying the hydrogen evolution thermodynamics, showing a thermodynamics-controlled characteristic. In contrast, for photoanodes (TiO and BiVO) with > 1 V, the bias required for cathode activation can be significantly reduced, exhibiting a kinetics-controlled characteristic.
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